Rapid Relief

Manufacturer
RAPID AID VIET NAM COMPANY LIMITED
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:38:07

Label at a glance#

ProductRapid Relief
Active ingredientMENTHOL
Label structure13 sections

Storage and handling

Store between 15-30℃(59-86℉) keep away from children

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Menthol 5% w/w.

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

Temporary relives of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

On wounds, cuts, damaged or infected skin
On eyes, mouth, genitals, or any other mucous membranes

If contact occurs, rinse thoroughly with water.

When using this product

OTC - WHEN USING SECTION

Use only as directed

Rear cases of serious burns have been reported with products of this type

Do not bandage tightly or use with a heating pad such as an electric heating pad, as this may result in excessive skin irritation or skin burn

Avoid contact with eyes and mucous membranes

Do not apply to wounds or damaged skin.

Do not use at the same time as other topical analgesics.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

Condition worsens

Redness is present

Irritation develops

Symptoms persist for more than 7 days or clear up and occur again within a few days

You experience signs of skin injury, such as pain, swelling or blistering where the product was applied as rare but the serious burns can occur.

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older:

Carefully remove backing from patch

Apply sticky side of patch to affected area.

Do not leave on skin for more than a total of 8 hours per day.

Repeat as necessary, but no more than 3 times daily .

Discard patch after single use.

Children under 12 years of age: do not use, consult a physician.

Supervise children when they use this product.

STORAGE AND HANDLING

STORAGE AND HANDLING SECTION

Store between 15-30℃(59-86℉) keep away from children

Inactive ingredients

INACTIVE INGREDIENT SECTION

Dihydroxyaluminum aminoacetate, DMDM hydantoin, Edetic acid, Glycerin, Isopropyl myristate, Polyacrylic acid, Polysorbate 80, Polyvinyl alcohol, Propylene glycol, Sodium polyacrylate, Tartaric acid, Titanium dioxide, Water

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83569-01083569-010-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4ca4a4a6-51a1-9acd-e063-6294a90abdb443499e6c-e77e-b994-e063-6394a90a61512026-03-10WarningsExact identifier
spl set id: 43499e6c-e77e-b994-e063-6394a90a6151